Institution
Incyte
Company•Wilmington, Delaware, United States•
About: Incyte is a company organization based out in Wilmington, Delaware, United States. It is known for research contribution in the topics: Expression vector & Ruxolitinib. The organization has 1262 authors who have published 1875 publications receiving 75015 citations. The organization is also known as: Incyte Corporation & Incyte Inc..
Topics: Expression vector, Ruxolitinib, Cancer, Polynucleotide, Antibody
Papers published on a yearly basis
Papers
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TL;DR: A potent CCR2 antagonist 21 (INCB3344) exhibited >100-fold selectivity over other homologous chemokine receptors, a free fraction of 24% in human serum and 15% in mouse serum, and an oral bioavailability of 47% in mice, suitable as a tool compound for target validation in rodent models.
35 citations
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TL;DR: The gene expression profiles indicate that ES cells actively suppress differentiation by transcriptional repression; cell-cell contact in embryoid bodies and retinoic acid treatment may overcome this suppression, allowing expression of Hox genes and inducing a suite of neuronal genes.
Abstract: Embryonic stem (ES) cells have the ability to differentiate into a variety of cell lineages. We are examining ES cell differentiation in vitro by using cDNA microarrays to generate a molecular phenotype for each cell type. El4 ES cells induced by retinoic acid after forming embryoid bodies differentiate almost exclusively to neurons. We obtained expression patterns for about 8500 gene sequences by comparing mRNAs from undifferentiated ES cells and their differentiated derivatives in a competitive hybridization. Our results indicate that the genes expressed by ES cells change dramatically as they differentiate (58 gene sequences up-regulated, 34 down-regulated). Most notably, totipotent ES cells expressed high levels of a repressor of Hox expression (the polycomb homolog Mphl) and a co-repressor (CTBP2). Expression of these genes was undetectable in differentiated cells; the ES cell-derived neurons expressed a different set of transcriptional regulators, as weil as markers of neurogenesis. The gene expression profiles indicate that ES cells actively suppress differentiation by transcriptional repression; cell-cell contact in embryoid bodies and retinoic acid treatment may overcome this suppression, allowing expression of Hox genes and inducing a suite of neuronal genes. Gene expression profiles will be a useful outcome measure for comparing in vitro treatments of differentiating ES cells and other stem cells. Also, knowing the molecule phenotype of transplantable cells will allow correlation of phenotype with the success of the transplant.
35 citations
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Sarah Cannon Research Institute1, University of Michigan2, Fox Chase Cancer Center3, University of Pittsburgh4, University of California, Davis5, University of Chicago6, University of Connecticut Health Center7, University of California, San Diego8, University of Colorado Denver9, Merck & Co.10, Incyte11
TL;DR: The immunosuppressive enzyme indoleamine 2, 3-dioxygenase 1 facilitates immune tolerance in cancer via T-cell suppression, and IDO1 overexpression is associated with poor tumorigenicity in mice.
Abstract: 3012Background: The immunosuppressive enzyme indoleamine 2, 3-dioxygenase 1 (IDO1) facilitates immune tolerance in cancer via T-cell suppression, and IDO1 overexpression is associated with poor sur...
35 citations
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TL;DR: Treatment with INCB018424 led to resolution of the symptoms of poor appetite and early satiety, along with the reduction in splenomegaly, which improves the nutritional status of MF patients.
35 citations
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18 Feb 2011TL;DR: In this paper, the present invention relates to cyclobutane and methylcyclobutanes derivatives, as well as their salts, compositions, and methods of use, which are Janus kinase (JAK) inhibitors useful in the treatment of JAK-associated diseases including, for example, inflammatory and autoimmune disorders, and cancer and myeloproliferative disorders.
Abstract: The present invention relates to cyclobutane and methylcyclobutane derivatives, as well as their salts, compositions, and methods of use, which are Janus kinase (JAK) inhibitors useful in the treatment of JAK-associated diseases including, for example, inflammatory and autoimmune disorders, as well as cancer and myeloproliferative disorders.
35 citations
Authors
Showing all 1267 results
Name | H-index | Papers | Citations |
---|---|---|---|
Patrick O. Brown | 183 | 755 | 200985 |
David Botstein | 165 | 468 | 212787 |
Inês Barroso | 113 | 301 | 76241 |
Alessandro M. Vannucchi | 94 | 715 | 35482 |
Ana M. Valdes | 84 | 334 | 26627 |
Mark C. Genovese | 79 | 364 | 26945 |
Michael B. Eisen | 71 | 170 | 89150 |
Jingyue Ju | 61 | 169 | 18952 |
Jeanne F. Loring | 60 | 177 | 14503 |
James Z. Wang | 57 | 225 | 21890 |
Emmett V. Schmidt | 50 | 150 | 9304 |
Günther Sperk | 50 | 124 | 10246 |
Robert C. Newton | 44 | 111 | 7369 |
Magnus Pfahl | 44 | 87 | 8064 |
William V. Williams | 44 | 168 | 7278 |